← Back to catalogue

Reflecto Femoral Augment Distal L.l./R.m Size 3 X 8 Mm

EUDAMED

Class III (EU MDR)

Ref 01.9837Model REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 8 MMRef 01.9825Model REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 4 MM

by Covision Medical Technologies Ltd.

Identity

Trade Name
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 8 MM EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 4 MM EUDAMED
Device Name
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 8 MM EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 4 MM EUDAMED
Model / Reference
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 8 MM EUDAMED
01.9837 EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 3 X 4 MM EUDAMED
01.9825 EUDAMED

Identifiers

Primary DI / UDI-DI
05051659178133 EUDAMED
05051659178010 EUDAMED
Basic UDI-DI
B-05051659178133 EUDAMED
B-05051659178010 EUDAMED
EMDN Code
P09098001 KNEE PROSTHESES AUGMENTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Reflecto Femoral Augment Distal L.l./R.m Size 3 X 8 Mm by Covision Medical Technologies Ltd. — Class III — MDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
GB-MF-000025081
Authorised Representative
Covision Medical Technologies (Ireland) Limited IE-AR-000031129

Sources (2)

  • EUDAMED 2a35d856-fecb-4f59-bde5-84dc00a41bfa 61 fields · synced Oct 6, 2026
  • EUDAMED da7024df-47be-47a1-9ca2-1f1d4e98e713 61 fields · synced May 18, 2026